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1 dritic (98%, 580/593), while 2% of them were axosomatic.
2 ural analysis revealed that CART establishes axosomatic and axodendritic contacts with CRH neurons in
3                              The patterns of axosomatic and axodendritic organization were determined
4 lls and their afferents through a complex of axosomatic and axodendritic synapses.
5 nucleus (ARC) males have twice the number of axosomatic and one-half the number of axodendritic spine
6 c vesicles were found both adjacent to IHCs (axosomatic) as well as apposed to afferent and efferent
7 tochondrial volume fraction were similar for axosomatic auditory nerve terminals, although rostral au
8 to mature granule neurons, were contacted by axosomatic, axodendritic and axospinous synapses.
9 scence confocal microscopy revealed numerous axosomatic, axodendritic, and axoaxonic contacts stained
10 aller ICNs of mouse lacked dendrites, formed axosomatic connections and had high synaptic efficacy co
11 tructural analyses revealed axodendritic and axosomatic contacts between PRV-labeled afferents and LC
12         Layers 5 and 6 were characterized by axosomatic contacts that displayed labeling in the presy
13 s compacta synapse mainly with dendrites and axosomatic contacts were not observed; (3) approximately
14                                    Symmetric axosomatic contacts were seen between SP-containing bout
15 taining numerous varicosities, indicative of axosomatic contacts.
16 ntacts, but some 5-HT-labeled terminals made axosomatic contacts.
17       Neurons of the cochlear nuclei receive axosomatic endings from primary afferent fibers from the
18 tical projection neurons, which have reduced axosomatic inhibitory synapses from the neuronal perikar
19 esynaptic protein complexin I is a marker of axosomatic (inhibitory) synapses, whereas complexin II i
20                  Patterns of distribution of axosomatic innervation in the lateral nucleus of the tra
21 shy cells received a different complement of axosomatic input compared to caudal bushy cells.
22 on between apical dendritic tuft, trunk, and axosomatic integration zones to control neuronal output
23               The increased firing caused by axosomatic Kv7 channel block backpropagated into distal
24 ial (RMP), amplified by control of intrinsic axosomatic membrane properties.
25 ings that demonstrate spikelet generation at axosomatic membranes.
26 -immunoreactive elements, but no evidence of axosomatic or axoaxonic degeneration in the adjacent gra
27         These newborn neurons do not receive axosomatic or axodendritic synapses indicating the absen
28 observations revealed septal boutons forming axosomatic or axodendritic type II synapses.
29 ely appose neuronal cell bodies and displace axosomatic presynaptic terminals.
30 ons, action potentials (APs) initiate in the axosomatic region and propagate into the dendritic tree
31 itive (PV(+)) interneurons, which target the axosomatic region of pyramidal cells, and the somatostat
32                               Boutons making axosomatic symmetric synapses in the granule cell layer
33 d < 20 microns) and a very high frequency of axosomatic synapses (> 20%).
34 a lucent cytoplasm and a higher frequency of axosomatic synapses (10.5% versus 3.7% for cholinergic n
35 ndant cytoplasm and organelles, and have few axosomatic synapses (both asymmetric and symmetric); (2)
36 e neuronal plasma membrane are juxtaposed to axosomatic synapses and associated with astrocytic proce
37 nificantly higher ratio of Glu-IR to GABA-IR axosomatic synapses and contained about twice as many da
38 e asymmetric, and the greatest percentage of axosomatic synapses between spindle afferents and trigem
39 IHC revealed the presence of axodendritic or axosomatic synapses between VIP-ir and PACAP-ir axon ter
40 ial nucleus (PBN) and consists of asymmetric axosomatic synapses containing calcitonin gene-related p
41  Control numbers of inhibitory Purkinje cell axosomatic synapses developed in the presence of the Trk
42         The ratio of labeled axodendritic to axosomatic synapses encountered was roughly consistent w
43                           The mean number of axosomatic synapses for these cells was three times that
44 al synaptic arrangements were observed: Main axosomatic synapses form between vesiculated endings and
45 ons and by their relatively large numbers of axosomatic synapses in comparison to esophageal motoneur
46 icroscopic data showing that many asymmetric axosomatic synapses in the BNST contain alpha(2A)-ARs.
47 eurons measured 39 x 29 microns and had 2-25 axosomatic synapses per somatic profile, representing an
48                            The proportion of axosomatic synapses was significantly higher in the late
49 axosomatic synapses, whereas, in the VM, the axosomatic synapses were rare, and 67% of nigral termina
50 while in the pars compacta of the PPN (PPNc) axosomatic synapses were rare.
51 ucture, dendritic arborization, and afferent axosomatic synapses), other features of the neuromuscula
52  full complement of Purkinje cell inhibitory axosomatic synapses, as defined ultrastructurally, and d
53 labeled terminals in the VAL was involved in axosomatic synapses, whereas, in the VM, the axosomatic
54 ely achieved through reduction of inhibitory axosomatic synapses.
55  in the cyprinid retina and may comprise all axosomatic synapses.
56 not increase the complement of Purkinje cell axosomatic synapses.
57 n GABA+ and GABA- cells, resembling cortical axosomatic synapses.
58 lu-rich neurons, which received only GABA-IR axosomatic synapses.
59  received axoaxonic and made axodendritic or axosomatic synaptic contacts.
60 ls called endbulbs of Held, which are large, axosomatic synaptic endings whose size and evolutionary
61 put through auditory nerve fibers via large, axosomatic synaptic terminals called the endbulbs of Hel
62                      The calyx of Held is an axosomatic terminal in the auditory brainstem that has a
63                 The calyx of Held is a giant axosomatic terminal in the auditory brainstem, whose bio
64 nucleus, utricular fibers formed a few large axosomatic terminals (spoon terminals) and a few small t
65 sults show that the proportion of inhibitory axosomatic terminals was significantly smaller in deaf a
66         By P10, large labeled terminals were axosomatic to OHCs and no longer found on IHCs.
67 th factor homologous factors (FHFs) bound to axosomatic voltage-gated sodium channels bear an N-termi